Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Amoxicillin for Oral Suspension USP Recalled by Teva Pharmaceuticals USA Due to Subpotency: due to a low, out of specification...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Teva Pharmaceuticals USA directly.
Affected Products
Amoxicillin for Oral Suspension USP, 125 mg per 5 mL, packaged in a 100 mL bottle, Rx only, Manufactured for: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960, NDC 0093-4150-73
Quantity: 133,601 bottles
Why Was This Recalled?
Subpotency: due to a low, out of specification test result for assay during stability testing.
Where Was This Sold?
United States and Puerto Rico
About Teva Pharmaceuticals USA
Teva Pharmaceuticals USA has 196 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report